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rs17662626

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs17662626(A;G)
Make rs17662626(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position193119895
is asnp
is mentioned by
dbSNPrs17662626
ebirs17662626
HLIrs17662626
Exacrs17662626
Varsomers17662626
Maprs17662626
PheGenIrs17662626
hapmaprs17662626
1000 genomesrs17662626
hgdprs17662626
ensemblrs17662626
gopubmedrs17662626
geneviewrs17662626
scholarrs17662626
googlers17662626
pharmgkbrs17662626
gwascentralrs17662626
openSNPrs17662626
23andMers17662626
23andMe allrs17662626
SNP Nexus

SNPshotrs17662626
SNPdbers17662626
MSV3drs17662626
GWAS Ctlgrs17662626
GMAF0.05418
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21926974OA-icon.png]
Trait
Title Genome-wide association study identifies five new schizophrenia loci.
Risk Allele A
P-val 5E-8
Odds Ratio 1.2000 [1.13-1.26]
GWAS snp
PMID [PMID 23453885OA-icon.png]
Trait Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)
Title Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
Risk Allele
P-val 5E-8
Odds Ratio NR NR


[PMID 23490065] A population-based association study of 2q32.3 and 8q21.3 loci with schizophrenia in Han Chinese